Good Laboratory Practice (GLP)

This GLP course is updated regularly to provide participants with current GLP trends and information.

This course is designed for staff working in the early phase drug development and commercial operations.

As the FDA states;

“Each individual engaged in the conduct of or responsible for the supervision of a nonclinical laboratory study shall have education, training, and experience, or combination thereof, to enable that individual to perform the assigned functions.”

Course Duration & Location

3-5 days, on your site or at one of our training centers.

CiPharma’s training courses can be delivered anywhere in the world. If your site is not in a city we have an office in then we ask you to cover the travel costs from our nearest office. You’ll save the costs associated with your staff travelling to be trained, so it becomes cost effective if you have several people needing training.

What you will learn

  • Understand the basics of GLP and basic good documentation practice
  • Be able to adopt GLP requirements into your daily work tasks and non-clinical projects
  • Have a relevant working knowledge of the ISO 17025 and OECD GLP principles
  • Know the roles and functions of key personnel within a GLP study
  • Be able to develop GLP compliant documentation
  • Understand the Quality Assurance Unit and its role in GLP management responsibilities in a GLP context

  • Course materials

    Participants will receive a copy of the presentation(s), relevant notes and workshop materials.
    A certificate of completion will be issued to participants who successfully complete the assessment.


    A written assessment is conducted at the end of the course.

    Course Format

    The course is a combination of lecture-style learning and active workshops with participants working in small groups on assigned tasks.

    Who should attend?

  • Quality Assurance / Quality Control personnel
  • Laboratory personnel
  • People new to the GxP regulated industries